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FDA 510(k)

SMR Lateralized Connectors with screws

K-Number: K183042 · 2019-01-25

Decision Date2019-01-25
Product CodeKWS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SMR Lateralized Connectors with screws is a medical device manufactured by Lima Corporate S.P.A.. It received FDA 510(k) clearance on 2019-01-25 under approval number K183042. The device is classified under product code KWS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SMR Lateralized Connectors with screws?

SMR Lateralized Connectors with screws is a medical device that received FDA 510(k) clearance on 2019-01-25. It is manufactured by Lima Corporate S.P.A.. The 510(k) number is K183042.

When was SMR Lateralized Connectors with screws approved by the FDA?

SMR Lateralized Connectors with screws received FDA 510(k) clearance on 2019-01-25, under approval number K183042.

What company makes SMR Lateralized Connectors with screws?

SMR Lateralized Connectors with screws is manufactured by Lima Corporate S.P.A..

What is the FDA product code for SMR Lateralized Connectors with screws?

The FDA product code for SMR Lateralized Connectors with screws is KWS.

Other Devices by Lima Corporate S.P.A.

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Related Devices (Code: KWS)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.